Characterization of language and reading skills in familial polymicrogyria
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2008
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Resumo |
Polymicrogyria (PMG) is a malformation of cortical development characterized by an excessive number of small gyri and abnormal cortical lamination, giving the cortical surface an irregular and gross appearance. The severity of clinical manifestations correlates with the extent of cortical involvement. The objective of the present study was to describe three families with linguistic features of developmental language disorder and reading impairment, and to establish a neuroanatomic correlation through neuroimaging. Subjects have been submitted to a comprehensive protocol including psychological assessment, language evaluation, neurological examination, and neuroimaging investigation. In our families, children usually had the diagnosis of developmental language disorder while adults had the diagnosis of reading impairment. MRI showed perisylvian polymicrogyria in several subjects of each family. Our data support the idea that there is a co-occurrence of developmental language disorder and reading impairment and both conditions may be associated with polymicrogyria. (c) 2007 Elsevier B.V. All rights reserved. |
Identificador |
BRAIN & DEVELOPMENT, v.30, n.4, p.254-260, 2008 0387-7604 http://producao.usp.br/handle/BDPI/26007 10.1016/j.braindev.2007.08.010 |
Idioma(s) |
eng |
Publicador |
ELSEVIER SCIENCE BV |
Relação |
Brain & Development |
Direitos |
restrictedAccess Copyright ELSEVIER SCIENCE BV |
Palavras-Chave | #developmental language disorder #reading impairment #polymicrogyria #malformation of cortical development #DEVELOPMENTAL DYSLEXIA #RISK #IMPAIRMENT #DISORDER #CHILDREN #Clinical Neurology |
Tipo |
article original article publishedVersion |